A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578388



Internal ID20951459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62871497..62872501hg38UCSC Ensembl
chr18:60538730..60539734hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245463
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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